Fortrea

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:The IT Data Analyst and Process Implementation intern role supports the ongoing development and optimization of an internal specific data dashboard and related database initiatives. The intern will use Python SQL and Power BI to transform clinical data enhance dashboard p

Job Overview:The IT Data Analyst and Process Implementation intern role supports the ongoing development and optimization of an internal specific data dashboard and related database initiatives. The intern will use Python SQL and Power BI to transform clinical data enhance dashboard p

Job Overview:The IT Internal Communications & Marketing Intern will collaborate with the IT Clinical Platforms Executive Director to support internal communications and technology adoption initiatives for the IT and Clinical Platforms organization. The intern will help design communic

Job Overview:The IT Internal Communications & Marketing Intern will collaborate with the IT Clinical Platforms Executive Director to support internal communications and technology adoption initiatives for the IT and Clinical Platforms organization. The intern will help design communic

Job Overview:The Data Quality Analyst intern will assist with regulatory compliance risk management and the implementation of the integral management system within clinical technology systems. Responsibilities include drafting and maintaining controlled documents contacting and follow

Job Overview:The Data Quality Analyst intern will assist with regulatory compliance risk management and the implementation of the integral management system within clinical technology systems. Responsibilities include drafting and maintaining controlled documents contacting and follow

Job Overview:The IT Clinical Configuration Operations & Management EDC/CTMS Intern will support the Clinical Technical Configuration Team by generating operational metrics consolidating data from multiple systems and preparing monthly team performance reviews. The intern will work wit

Job Overview:The IT Clinical Configuration Operations & Management EDC/CTMS Intern will support the Clinical Technical Configuration Team by generating operational metrics consolidating data from multiple systems and preparing monthly team performance reviews. The intern will work wit

We are looking for a Clinical StartUp Contract & Finance Specialist to support clinical trial startup activities across Austria. This role is an excellent opportunity for professionals with experience in clinical startup operations budget/contract negotiations and regulatory processes

We are looking for a Clinical StartUp Contract & Finance Specialist to support clinical trial startup activities across Austria. This role is an excellent opportunity for professionals with experience in clinical startup operations budget/contract negotiations and regulatory processes

Job Overview:We are seeking an experienced Workday Configuration Analyst with deepexpertisein Record-to-Report (R2R) modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that enableaccuratefinancial rep

Job Overview:We are seeking an experienced Workday Configuration Analyst with deepexpertisein Record-to-Report (R2R) modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that enableaccuratefinancial rep

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tool Medidata RAVE. Develop/validate Custom datasets (CF) and efficiently handle external data and reconciliations. Perform any postproduction changes to th

Job Overview:Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tool Medidata RAVE. Develop/validate Custom datasets (CF) and efficiently handle external data and reconciliations. Perform any postproduction changes to th

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs). Data entry of safety data onto adverse event tracking systems. Write patient narratives & code a

The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs). Data entry of safety data onto adverse event tracking systems. Write patient narratives & code a

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process ex

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process ex

Exciting opportunity to be part of the Fortrea India Apprentice Program!As a Fortrea Apprentice you will have the opportunity to support meaningful assignments that compliment an education in STEM Business and Healthcare disciplines and are inspiring and valuable in our mission to imp

Exciting opportunity to be part of the Fortrea India Apprentice Program!As a Fortrea Apprentice you will have the opportunity to support meaningful assignments that compliment an education in STEM Business and Healthcare disciplines and are inspiring and valuable in our mission to imp

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

Our Clinical Operations department in the UK is seeking a SCRA II to work across a variety of therapeutic areas including Oncology. While you can be based anywhere in the UK previous UK monitoring experience is essential. Experience in Ophthalmology would be considered an asset.The r

Our Clinical Operations department in the UK is seeking a SCRA II to work across a variety of therapeutic areas including Oncology. While you can be based anywhere in the UK previous UK monitoring experience is essential. Experience in Ophthalmology would be considered an asset.The r

London 23 days onsite (hybrid)Are you a regulatoryfocused Study StartUp expert who thrives on ownership and compliance Were looking for a Study StartUp PM to lead countrylevel submissions approvals and site readiness for a global clientdedicated program.What youll ownOversight of en

London 23 days onsite (hybrid)Are you a regulatoryfocused Study StartUp expert who thrives on ownership and compliance Were looking for a Study StartUp PM to lead countrylevel submissions approvals and site readiness for a global clientdedicated program.What youll ownOversight of en

The Strategic Deals and Partnerships role will have global responsibility for driving strategic partnerships across biopharma accounts and other key organizations including financial entities supporting clinical trial funding. This position leads cross-functional Deal Teams to design

The Strategic Deals and Partnerships role will have global responsibility for driving strategic partnerships across biopharma accounts and other key organizations including financial entities supporting clinical trial funding. This position leads cross-functional Deal Teams to design

Job Overview:Were seeking a Solutions Architect to design and guide endtoend solutions across our Corporate Systems portfolio (Finance HR Procurement Corporate Systems). Youll partner with business and technology leaders to translate strategy and requirements into secure scalable arch

Job Overview:Were seeking a Solutions Architect to design and guide endtoend solutions across our Corporate Systems portfolio (Finance HR Procurement Corporate Systems). Youll partner with business and technology leaders to translate strategy and requirements into secure scalable arch

Job Overview:Responsible for Medical Writing activities such as appendices collation peer review and QC and publishing for designated projects and to ensure quality and compliance with Fortrea or Sponsors SOPs ICH GCP and regulatory requirements.Summary of Responsibilities:Assist with

Job Overview:Responsible for Medical Writing activities such as appendices collation peer review and QC and publishing for designated projects and to ensure quality and compliance with Fortrea or Sponsors SOPs ICH GCP and regulatory requirements.Summary of Responsibilities:Assist with

Job Overview:Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis.Summary of Responsibilities:Provide programming support for analysis of real-wor

Job Overview:Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis.Summary of Responsibilities:Provide programming support for analysis of real-wor

Job Overview:Responsible for reviewing clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to ensure documents are accurate consistent grammatically correct well written and logical by providing review comments and docum

Job Overview:Responsible for reviewing clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to ensure documents are accurate consistent grammatically correct well written and logical by providing review comments and docum